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Human Psychopharmacology|July 22, 2014
Effect of polymorphisms on the pharmacokinetics, pharmacodynamics, and safety of risperidone in healthy volunteersTeresa Cabaleiro, Dolores Ochoa, Rosario López-Rodríguez, et al.
Medicina Clinica|November 13, 2010
[Holt-Oram syndrome: study of 7 cases]Mónica Martínez-García, Isabel Lorda-Sanchez, Maria García-Hoyos, et al.
Molecular Vision|February 10, 2010
New mutations in BBS genes in small consanguineous families with Bardet-Biedl syndrome: detection of candidate regions by homozygosity mappingInes Pereiro, Diana Valverde, Teresa Piñeiro-Gallego, et al.
Prenatal Diagnosis|August 10, 2005
Trisomy 2 due to a 3:1 segregation in an abortion studied by QF-PCR and CGHIsabel Lorda-Sánchez, Dan Diego-Alvarez, Carmen Ayuso, et al.
Radiographics : a Review Publication of the Radiological Society of North America, Inc|May 19, 2009
Role of 3.0-T MR colonography in the evaluation of inflammatory bowel diseaseJordi Rimola, Sonia Rodríguez, Orlando García-Bosch, et al.
Epilepsy Research|December 4, 2003
Characterization of a 6p21 translocation breakpoint in a family with idiopathic generalized epilepsyLaura Sáez-Hernández, Belén Peral, Raúl Sanz, et al.
Hepatology (Baltimore, Md.)|November 27, 2004
Initial response to percutaneous ablation predicts survival in patients with hepatocellular carcinomaMargarita Sala, Josep M Llovet, Ramon Vilana, et al.
Ophthalmic Genetics|September 27, 2007
Screening of the USH1G gene among Spanish patients with Usher syndrome. Lack of mutations and evidence of a minor role in the pathogenesis of the syndromeElena Aller, Teresa Jaijo, Magdalena Beneyto, et al.
Molecular Vision|April 15, 2009
ABCA4 mutations in Portuguese Stargardt patients: identification of new mutations and their phenotypic analysisSusana Maia-Lopes, Jana Aguirre-Lamban, Miguel Castelo-Branco, et al.
Stem Cell Research|October 27, 2018
Generation of a human iPSC line from a patient with Leber congenital amaurosis caused by mutation in AIPL1Dunja Lukovic, Ana Artero Castro, Marian León, et al.
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